Analyst I, QC Laboratory Services

The Analyst I will perform GMP-compliant testing to support in-process testing, finished product release, and stability programs, including nonclinical/clinical studies and assay or process validations.

Requirements

• University degree or technical diploma in biochemistry, biology, microbiology, or related field of study
• 0-2 years directly related experience in a recognized professional or technical/scientific field and experience in a pharmaceutical cGMP or regulated environment
• Basic knowledge of Microsoft Office - Word, Excel
• Basic knowledge of pharmaceutical GMPs
• Knowledge of laboratory techniques and safety precautions
• WHMIS and biohazard safety awareness
• Proficient in laboratory safety and good laboratory practices (GLP), including maintaining complete and accurate written laboratory records
• Previous experience with LIMS, Veeva and SAP is considered an asset
• Willingness to work off-schedule shifts to support in-process manufacturing
• Able to communicate and articulate information in both written and verbal forms
• Strong organizational and interpersonal skills; can work collaboratively with others
• Able to interpret analytical data
• Able to contribute ideas/solutions to aid in troubleshooting and investigations
• Able to work in a fast-paced, high-throughput environment and adapt to change, particularly in schedule
• Able to lift up to 25 lbs
• Successful completion of Emergent security clearance and a pre-employment medical is required

Benefits

• Competitive salaries
• Flexible work arrangements
• Extensive benefits package